A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521426



Internal ID15102033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:2661619..2666244hg38UCSC Ensembl
Innerchr6:2661853..2666478hg19UCSC Ensembl
Innerchr6:2606852..2611477hg18UCSC Ensembl
Innerchr6:2606852..2611477hg17UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384626
hg194626
hg184626
hg174626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698034
Samples
Known GenesMYLK4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521426
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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